• 제목/요약/키워드: Spiking fever

검색결과 8건 처리시간 0.018초

지속적인 고열을 동반한 폐렴양 결핵병변 1예 (A Case of Tuberculous Pneumonitis With Continuous High Spiking Fever)

  • 차봉수;김세규;이홍열;장준;김성규;이원영
    • Tuberculosis and Respiratory Diseases
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    • 제41권3호
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    • pp.302-306
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    • 1994
  • A 33-year old male was admitted due to continuous high spiking fever for 2 months via local clinic. He had been diagnosed pulmonary tuberculosis at local clinic. However, spiking fever had not been controlled by anti-tuberculous medications. Chest PA showed confluent consolidation on right upper & mid-lung field. 5 anti-tuberculous regimens(Streptomycin, Isoniazid, Rifampin, Ethambutol, Pyrazinamaide) were administered initially and steroid therapy was followed for relieving toxic symptoms Very slowly resolved chest X-ray lesion and continuous fever suggested the possibility of misdiagnosis. After 60th hospital day, the chest X-ray lesion was resolved gradually and fever subsided almost completely. He was discharged on 76th hospital day with anti-tuberculous drugs and steroid(prednisolon), without any other problems except sustained mild fever.

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폐실질내 기형종 -1례 보고- (Intrapulmonary teratoma -Report of a case-)

  • 박도웅
    • Journal of Chest Surgery
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    • 제22권1호
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    • pp.158-162
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    • 1989
  • This paper reports a case in a 16-year-old female of intrapulmonary teratoma located in the right upper and middle lobes of the lung. The initial symptoms were high spiking fever, cough and chest pain. Initial chest X-ray revealed large homogenous mass in the right upper and middle lung fields. So intercostal tube drainage was done under the impression of the lung abscess. But mass density was remained on the follow-up chest X-ray, the patient had resection of the right upper and middle lobes of the lung. The gross and microscopic findings of the resected specimen revealed characteristic findings of the intrapulmonary teratoma. The patient is asymtomatic at present and living a normal life.

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성인 발병성 스틸병(Adult-onset Still's disease)으로 오인된 전신홍반루푸스(Systemic Lupus Erythematosus) 1예 (A Case of Systemic Lupus Erythematosus Misdiagnosed as Adult-onset Still's Disease)

  • 오명진;김현제;이한솔;허지안;홍영훈;이충기
    • Journal of Yeungnam Medical Science
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    • 제27권1호
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    • pp.78-84
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    • 2010
  • Adult-onset Still's disease (AOSD) is an inflammatory disorder that's characterized by daily, spiking high fever, arthritis and an evanescent, salmon-pink rash. AOSD is diagnosed purely on the basis of the typical clinical features of the illness. The symptoms commonly include swelling of the lymph nodes, enlargement of the spleen and liver, and a sore throat. AOSD is difficult to differentiate from systemic lupus erythematosus (SLE) due to the similar clinical manifestations. We report here on a case of a 16-year-old female patient with autism and epilepsy and who complained of daily spiking fever for 20 days. The patient had maculopapular skin rashes on the face and whole body and lymphadenopathy. The liver function tests were elevated mildly. The initial rheumatoid factor (RF) and antinuclear antibody (ANA) tests were negative. We diagnosed her as having adult-onset Still's disease according to the criteria of Yamaguchi. We successfully treated her with oral prednisolone. But her antinuclear antibody test was changed to positive after discharge. So we finally diagnosed her as having SLE.

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마이코플라즈마 폐렴 환아에서 병발한 가와사키병 1례 (A Case of Kawasaki Disease with Mycoplasma Pneumonia)

  • 이세민;박소은;김연우;홍정연
    • Clinical and Experimental Pediatrics
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    • 제48권4호
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    • pp.438-442
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    • 2005
  • 우리나라에서는 아직 마이코플라스마 폐렴이 가와사키병에 병발한 경우가 보고된 적이 없으며 마이코플라스마 폐렴의 특성상 다양한 호흡기 외의 증상이 비교적 흔하게 동반되는 점 등을 고려할 때, 적절한 치료에도 불구하고 지속되는 발열을 보이는 마이코플라스마 폐렴의 경우 반드시 비전형적 가와사키병이 감별되어야 할 것이며, 이미 언급한 바와 같이 초항원(superantigen)에 근거해 가와사키병의 병태생리를 규명하고자 하는 연구들을 지지할 수 있는 또 하나의 근거로 생각되어 본 증례를 보고하는 바이다.

심내막염 환자의 동종이식편 치환술 -1례 보고- (Homograft Replacement in Prosthetic Valve Endocarditis(PVE) -One Case Report)

  • 박중원;박국양;김웅한
    • Journal of Chest Surgery
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    • 제30권8호
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    • pp.815-818
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    • 1997
  • 인공판막심내막염은 드물지만 합병증으로 판막주위가 감염으로 파괴되고 농양이 형성되는 경우가 있어 높 은 사망율을 가져온다. 그러나 적절한 항생제의 사용, 심장초음파 검사에 기초를 둔 조기 진단,수술시 효과적인 심근보호. 그리고 수술경험의 축적으로 인공판막심내막염에 있어서 보다좋은 장단기 결과를 얻을 수 있다. 35세 남자 환자가 94년 8월에 대동맥판막, 승모판막대치술과 함께 삼첨판륜성형술을 받은후 특별한 증상 없이 지내다가 갑자기 시작된 실어증, 양안구의 좌측편위, 고열로 입원하여 심장초음파 검사를 시행한 결과 인공판막 심내막염 소견을 보여 6주간의 항생제 치료후 수술을 시행하였다. 수술소견상 대동맥 판륜을 따라 증식물 소견과 판막 주위의 누출, 농양주머니가 형성되어 있었고 승모판막은 비교적 건강해 보였다. 수술은 감염된 조직의 전체적인 제거와 냉동저장된 대동맥 동종이식편을 이용하여 재대치 수술을 시행했다. 환자는 수술후 63일째 퇴원했으며 퇴원후 7개월 동안 외래 추적 관찰결과 특별한 이상소견 없이 지내고 있다.

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Atypical Hemolytic Uremic Syndrome after Traumatic Rectal Injury: A Case Report

  • Kang, Ji-Hyoun;Lee, Donghyun;Park, Yunchul
    • Journal of Trauma and Injury
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    • 제34권4호
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    • pp.299-304
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    • 2021
  • Atypical hemolytic uremic syndrome (aHUS) is a rare, progressive, life-threatening condition of thrombotic microangiopathy characterized by thrombocytopenia, microangiopathic hemolytic anemia, and renal impairment. The mechanisms underlying aHUS remain unclear. Herein, we present the first case in the literature of aHUS after a traumatic injury. A 55-year-old male visited the emergency department after a traumatic injury caused by a tree limb. Abdominal computed tomography revealed a rectal wall defect with significant air density in the perirectal space and preperitoneum, implying rectal perforation. Due to the absence of intraperitoneal intestinal perforation, we performed diverting sigmoid loop colostomy. An additional intermittent simple repair was performed due to perianal and anal injuries. One day postoperatively, his urine output abruptly decreased and serum creatinine level increased. His platelet level decreased, and a spiking fever occurred after 2 days. The patient was diagnosed with acute renal failure secondary to aHUS and was treated with fresh frozen plasma replacement. Continuous renal replacement therapy (CRRT) was also started for oliguria and uremic symptoms. The patient received CRRT for 3 days and intermittent hemodialysis thereafter. After hemodialysis and subsequent supportive treatment, his urine output and renal function improved. The hemolytic anemia and thrombocytopenia also gradually improved. Dialysis was terminated on day 22 of admission and the patient was discharged after recovery. This case suggests that that a traumatic event can trigger aHUS, which should be considered in patients who have thrombocytopenia and acute renal failure with microangiopathic hemolytic anemia. Early diagnosis and appropriate management are critical for favorable outcomes.

다제내성 결핵환자에서 Prothionamide에 의한 급성 간염 1예 (A Case of Prothionamide Induced Hepatitis on Patient with Multi-Drug Resistant Pulmonary Tuberculosis)

  • 박준범;박병훈;손지영;정지예;김은영;임주은;이상훈;이상국;김송이;정원재;임승택;이경종;강영애;김영삼;김세규;장준;최준정;박무석
    • Tuberculosis and Respiratory Diseases
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    • 제70권3호
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    • pp.251-256
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    • 2011
  • The prevalence of multi-drug resistant tuberculosis (MDR-TB), which is resistant to isoniazid and rifampin, has been increasing in Korea. And the side effects of 2nd line anti-tuberculosis medications, including drug-induced hepatitis, are well known. Although prothionamide (PTH) is one of the most useful anti-TB medications and although TB medication-induced acute hepatitis is a severe complication, there are only a few published case reports about prothionamide induced hepatitis. In this case report, a 22 year old male was diagnosed with pulmonary MDR-TB and was administered 2nd line anti-TB mediations, including PTH. Afterwards, he had a spiking fever and his liver enzymes were more than 5 times greater than the upper limit of the normal range. He was then diagnosed with drug-induced hepatitis by liver biopsy. His symptoms and liver enzyme elevation were improved after stopping PTH. Accordingly, we report this case of an association between PTH and acute hepatitis.

저산소증으로 미만성 뇌피질 손상이 유발된 성인형 스틸병 환아(患兒) 1례(例) 보고(報告) (The Clinical Study on 1 Case of Patient with Adult-onset Still's Disease who had a Diffuse Cerebral Dysfunction developed after Hypoxia. (A case of Adult-onset Still's Disease and Diffuse Cerebral Dysfunction))

  • 송인선;신지나;송미진;이정림
    • 대한한방소아과학회지
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    • 제17권2호
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    • pp.15-26
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    • 2003
  • 저자는 류마티스 관절염의 일종인 성인형 스틸병으로 치료받던 16세 환아의 치료 과정 중 발생한 미만성 뇌피질 손상 1예(例)에 대하여 초기 양방 병원에서의 치료에도 변화가 없었던 운동마비와 정신신경계통의 제반 증상에 대하여 한방적 치료한 결과 호전도가 있었기에 증예보고(證例報告)하는 바이다. 특히 경계정충(驚悸??)을 동반한 불면(不眠)에 대하여 자하차(紫河車) 약철(藥鍼)과 녹용(鹿茸) 약철(藥鍼)을 시술한 것에 대하여서는 지견을 얻었으며 가미온담탕(加味溫膽湯), 양심탕류(養心湯類)의 처방이 유용한 효과가 있다는 결론을 얻었다. 하지만 150일이라는 장기입원 치료에 비해서 전실어(全失語)는 거의 호전을 보지 못했으며 Mental Grade가 GCS 상 12점까지 상승하였으나 일상생활에서의 능동적인 운동능력의 호전에는 한계가 있었다는데서 아쉬움이 남는다. 아직까지 한방 분야에서 성인형 스틸병과 미만성 뇌피질 손상에 대한 연구는 별로 보고된 것이 없었으며, 특히 장기간의 관리가 필요한 마비 질환의 경우 그 평가 척도나 정신계통의 회복에 있어서 연구 및 치료방법이 부족한 듯하며 차후 지속적인 연구가 필요하리라 사료된다.

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